FDA issued a Warning Letter to Genzyme Corporation on 2/27/2009 as a result of this inspection.
FDA investigators audited the Sanofi Genzyme - Allston, MA, United States facility and issued inspectional observations (via FDA 483) on 10 Oct 2008.
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- Category: Human Drugs
- Inspection end: 10 Oct 2008
- Location: Allston, United States
- FEI: 1000305672